Feasibility study of a short Bevacizumab infusion in patients.

Feasibility study of a short Bevacizumab infusion in patients. - Feasibility study of a short Bevacizumab infusion in patients.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000018293

Enrollment

Registered

2015-07-21

Start date

2015-06-01

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

colorectal cancer,breast cancer,ovarian cancer, lung cancer, cervical cancer

Interventions

Bevacizumab is administered in 0.5mg/kg/min.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1)meet the administration criteria of bevacizumab 2)outpatients 3)Age 20 years and above 4)ECOG PS 0-2 5)No prior therapy of bevacizumab 6)Written informed consent

Exclusion criteria

Exclusion criteria: 1)Systemic administration of corticosteroids 2)Patients whose participation in the trial is judged to be inappropriate by the attending doctor

Design outcomes

Primary

Measure	Time frame
Having onset of hypersensitivity reaction or not	—

Secondary

Measure	Time frame
grade of infusion related reaction(CTCAE v.4.0),feasibility	—

Countries

Japan

Contacts

Public ContactAkiko Konomatsu

NIPPON MEDICAL SCHOOL MUSASHI KOSUGI HOSPITAL Pharmacy

akk-koo@nms.ac.jp044-733-5181

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026